Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report

BACKGROUND: Recent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). The clinical characteristics of hereditary PPGL are varying among the types of mutational genes. It is still difficult to specify the pathognomonic symptoms in the...

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Detaylı Bibliyografya
Yayımlandı:Surg Case Rep
Asıl Yazarlar: Shibata, Masahiro, Inaishi, Takahiro, Miyajima, Noriyuki, Adachi, Yayoi, Takano, Yuko, Nakanishi, Kenichi, Takeuchi, Dai, Noda, Sumiyo, Aita, Yuichi, Takekoshi, Kazuhiro, Kodera, Yasuhiro, Kikumori, Toyone
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer Berlin Heidelberg 2017
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5745210/
https://ncbi.nlm.nih.gov/pubmed/29282558
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-017-0408-x
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